ZMP
DPEP2
Ensembl ID:
Description:
dipeptidase 2 [Source:HGNC Symbol;Acc:23028]
Human Orthologues:
DPEP2, DPEP3
Human Descriptions:
dipeptidase 2 [Source:HGNC Symbol;Acc:23028]
dipeptidase 3 [Source:HGNC Symbol;Acc:23029]
dipeptidase 3 [Source:HGNC Symbol;Acc:23029]
Mouse Orthologues:
Dpep2, Dpep3
Mouse Descriptions:
dipeptidase 2 Gene [Source:MGI Symbol;Acc:MGI:2442042]
dipeptidase 3 Gene [Source:MGI Symbol;Acc:MGI:1919104]
dipeptidase 3 Gene [Source:MGI Symbol;Acc:MGI:1919104]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38625 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40949 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38625
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113842 | Essential Splice Site | 47 | 425 | 1 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 36723701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 34997544 |
GRCz11 | 7 | 35269021 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCAGTAGAGCCCTGGATATGATGACAAAATATCCACTAATTGATGGG[T/A]AGGACACACTTTTCACTGTATGGCTTTCTGAAAATAATTAATTGCAAATA
Long Flanking Sequence:
AGATACAACAGATATTAGTCTGCATATAAATAAGTGATTTTATATGTGGTCTGTGAGTTTGATGAAAATCTTTTACGGTAAAAATAACAATTACAGCAATAATAATAAACAGAAAGTTTATTTATTTACTTTTTCATTCATTTATTTATTTATTATTATTTTTTCTCTCTCTAACTTTTGTTACAGAAAAAATCATACTTTTGAAAACAGCACTTATGACAACATGAATCCTTAAACAGCTATTTACACAAAGAAATCTGATGCAAGTAGCCCATTATATTTATTTTAAACATTTTTCATGGGCATGCTAGTTGCTGGTAAATTCTGCATATTTGAAGTCAAATTCTTCATGACATAGAATGTTAATACATAAAGAAGCAGGCATCAGTGGGGCATGGCTACAGTGGTTCATATGCATCAGTCTCTCACTTCTTCATGGAGTCATATCGGAAACCAGTAGAGCCCTGGATATGATGACAAAATATCCACTAATTGATGGG[T/A]AGGACACACTTTTCACTGTATGGCTTTCTGAAAATAATTAATTGCAAATAACTTCAGAATAAAGTAGTAATTGGCAACATTTTTTTTAAAAAAGTAAAAATGTATAAAAAGTGATTTATTGTGATTTCCTATGCTTCTTTTTCTCTTTTGTCAGACACAATGACTGGGCACTACACTTGAGAAAACATGATGACAACAAACTAACAAAGGTTAATCTCTACAATTATCCTCAGGGGGCTACAGATATCACTCGCCTCATTGCTGGCCATGTTGGAGGTCAGGTAAATTCTCCTACTTTATCCTGATTCTGATTTATGTTTTTAAAATATTCAGTAGCGTGACCTGCTTCTAACTATTATTTGCGAGTTAAACCAATTTCAAACTCACAAAGGTCATAGCCTATATTTGTTTTTATCTGAAATTGTGGTAGTAGACCAATAAGATAAAACTGAAACAGCATATTAAAAATAGTGCTGTTAATGCTTTTTTAATTTAGCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40949
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113842 | Splice Site, Nonsense | 203 | 425 | 5 | 10 |
Genomic Location (Zv9):
Chromosome 7 (position 36727994)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 35001837 |
GRCz11 | 7 | 35273314 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTTTATCAACATTACCAGTGGGTGAACAACAGCCTGACAGAATTTGGC[A/T]AGGTAATATTCTTTCTGGATGGATTGATGGTAAATAAAACTATGTAAAAC
Long Flanking Sequence:
TCCAGGTGCTCCCATTTCCCCCACAGTACAAAAACATGCTATAGGTAAAATCGGATAAACCAAATTGTCATGTATAGGATTATATAAAAACACTTTTCTACATTGTGCTTTTTCTACATAGTGTGTGTAAGAAAATACATGTTTTTCTATTTATTTGTTTGTTTCATCTGTTTTGTTTTGTCTTGTTATGCATTTTAGGAATGAAGAAGAGTACAAAAATTGCATGTCTAATCAGTGTGGAGGGAGGCCACTCCATTGACAGCAGTTTAGCAGCTCTACGCATGTTTTACCAGCTCGGCGTGAGATCCATGAGTCTCACACACACCTGCAACACACCGTGGTAAATACTCAACATACCAAACAAATTACTGTCATTTAGACATACTGCCATTTAGATCAATACTTACCATTTCTCTAATGATGTCACACATAGGGCAAAGAGCTCATCTAGTTTTTATCAACATTACCAGTGGGTGAACAACAGCCTGACAGAATTTGGC[A/T]AGGTAATATTCTTTCTGGATGGATTGATGGTAAATAAAACTATGTAAAACAAAACAGACCGCACTGAAAGATAAAGGTTAATGAACCAATAAAGTTGAAAGAAGTACAGTTATATTTAGGGAATTATTTGTCCTCTTCCTTCATCCACTTCTATATTTGGAAACCACTTTCTTGTGTCTCAGTTTTGAACCCCAAGGCTGGAATTACTGGAAGTTCAAATCTGTTTTCTTTTTGCTTAAGCAAAACAAAATCTGGGAGTTTTGCATTTTTTGTATGGAATTTTTGTATTTATTTGACTTGAGTTACAATTTCTGACAGATCCAAACATACAAATGGCAAGTTCATTTATACAGCACATATCATACACAATGGTAATTCAAAGTGCTTTGCATAAACAGGAATAAAATGGTGATAGCAAATATCTGTTTTATTGATTTAGAATGGGGCGACACAGTGGCGCAGTAGGTAGTGCTGTCGCCTCATAGCAAGAGGGTAGCTGG
Associated Phenotype:
Not determined